1. Diseases
  2. Weissenbacher- Zweymuller syndrome

Weissenbacher- Zweymuller syndrome

Disease Export to PDF
Name:
Weissenbacher- Zweymuller syndrome
Description:
Weissenbacher-Zweymuller syndrome (WZS) is characterized by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.
ORPHAcode:
3450
Synonyms:
Heterozygous OSMED
Heterozygous otospondylomegaepiphyseal dysplasia
Pierre Robin sequence-fetal chondrodysplasia syndrome
Pierre Robin syndrome-fetal chondrodysplasia syndrome
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
COL11A2
COL2A1
Created:
13 May 2019 - 01:02
Changed:
01 Jul 2019 - 06:57